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Vital Pulp Therapy to Treat Irreversible Pulpitis (VPT)

S

Shahid Beheshti University of Medical Sciences

Status

Completed

Conditions

Pulpitis

Treatments

Procedure: pulpotomy
Procedure: One-visit root canal therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT00748280
C/B/4/8253

Details and patient eligibility

About

The purpose of this study is to demonstrate non-inferiority of pulpotomy treatment (with new endodontic bio-materials) as a new treatment with one-visit root canal therapy as reference treatment in pain relief and clinical and radiographic success, for irreversible pulpitis of human permanent molar teeth.

Full description

In one visit RCT (Arm 1): The teeth were anesthetized, isolated and endodontic access and instrumentation of all canals was done. Canal preparation was conducted using a step-back technique. The working lengths were determined and confirmed by radiography. Sterile normal saline solution was used for intra-canal irrigation. Root canals were obturated with gutta-percha and sealer using lateral condensation technique. After placing a cotton pellet in the pulp chamber, the access cavity was closed with Cavit.

In pulpotomy treatment with CEM/MTA (Arm 2): The teeth were anesthetized. Pulpotomy procedure of removing inflamed pulp tissue to the stump level was done. Homeostasis was achieved by irrigating the cavity with sterile normal saline and application of small pieces of sterile cotton pellets. The pulpal wound was covered with an approximately 2-mm-thick layer of MTA/CEM cement. Pulp chambers were then covered with a wet cotton pellet and sealed with Cavit.

Enrollment

615 patients

Sex

All

Ages

9 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Diagnostic criteria:

    1. Patient reports pain of endodontic origin
    2. Diagnosis of irreversible pulpitis
  • Eligibility criteria:

    1. Molar tooth
    2. Patient chooses to have tooth extraction for pain relief
    3. Age 9-65 years
    4. Both gender
    5. The patient had read and thoroughly understood the questionnaires; and
    6. Written informed consent
  • Exclusion Criteria:

    1. Moderate or severe periodontitis
    2. None restorable tooth
    3. Internal or external root resorption
    4. Root canal calcification
    5. No bleeding after access cavity preparation
    6. Analgesic taken within the last 4 h
    7. Active systemic disease
    8. The patient was pregnant or nursing
    9. History of opioid addiction or abuse
    10. Temporary residency

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

615 participants in 2 patient groups

1
Experimental group
Description:
ORCT
Treatment:
Procedure: One-visit root canal therapy
2
Experimental group
Description:
PCEM/PMTA
Treatment:
Procedure: pulpotomy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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